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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/725
Title: Directly-observed therapy (DOT) for the radical 14-day primaquine treatment of Plasmodium vivax malaria on the Thai-Myanmar border
Authors: Takeuchi, Rie
Saranath Lawpoolsri
สารนาถ ล้อพูลศรี
Mallika Imwong
มัลลิกา อิ่มวงศ์
Kobayashi, Jun
Jaranit Kaewkungwal
จรณิต แก้วกังวาล
Sasithon Pukrittayakamee
ศศิธร ผู้กฤตยาคามี
Supalap Puangsa-art
ศุภลาภ พวงสอาด
Nipon Thanyavanich
นิพนธ์ ธัญญวานิช
Wanchai Maneeboonyang
วรรณไชย มณีบุญยัง
Day, Nicholas P.J.
Pratap Singhasivanon
ประตาป สิงหศิวานนท์
Mahidol University. Faculty of Tropical Medicine. Department of Clinical Tropical Medicine
Mahidol University. Faculty of Tropical Medicine. Mahidol-Oxford Tropical Medicine Research Unit (MORU)
Mahidol University. Faculty of Tropical Medicine. Department of Tropical Hygiene.
Pratap Singhasivanon
Keywords: Antimalarials;Directly observed therapy;Humans;Malaria, Vivax;Primaquine;Open Access article
Issue Date: 1-Nov-2010
Citation: Takeuchi R, Lawpoolsri S, Imwong M, Kobayashi J, Kaewkungwal J, Pukrittayakamee S. et al. Directly-observed therapy (DOT) for the radical 14-day primaquine treatment of Plasmodium vivax malaria on the Thai-Myanmar border. Malar J. 2010 Nov 1;9:308.
Abstract: BACKGROUND: Plasmodium vivax has a dormant hepatic stage, called the hypnozoite, which can cause relapse months after the initial attack. For 50 years, primaquine has been used as a hypnozoitocide to radically cure P. vivax infection, but major concerns remain regarding the side-effects of the drug and adherence to the 14-day regimen. This study examined the effectiveness of using the directly-observed therapy (DOT) method for the radical treatment of P. vivax malaria infection, to prevent reappearance of the parasite within the 90-day follow-up period. Other potential risk factors for the reappearance of P. vivax were also explored. METHODS: A randomized trial was conducted from May 2007 to January 2009 in a low malaria transmission area along the Thai-Myanmar border. Patients aged ≥ 3 years diagnosed with P. vivax by microscopy, were recruited. All patients were treated with the national standard regimen of chloroquine for three days followed by primaquine for 14 days. Patients were randomized to receive DOT or self-administered therapy (SAT). All patients were followed for three months to check for any reappearance of P. vivax. RESULTS: Of the 216 patients enrolled, 109 were randomized to DOT and 107 to SAT. All patients recovered without serious adverse effects. The vivax reappearance rate was significantly lower in the DOT group than the SAT group (3.4/10,000 person-days vs. 13.5/10,000 person-days, p = 0.021). Factors related to the reappearance of vivax malaria included inadequate total primaquine dosage received (< 2.75 mg/kg), duration of fever ≤ 2 days before initiation of treatment, parasite count on admission ≥ 10,000/µl, multiple P. vivax-genotype infection, and presence of P. falciparum infection during the follow-up period. CONCLUSIONS: Adherence to the 14-day primaquine regimen is important for the radical cure of P. vivax malaria infection. Implementation of DOT reduces the reappearance rate of the parasite, and may subsequently decrease P. vivax transmission in the area.
URI: http://repository.li.mahidol.ac.th/dspace/handle/123456789/725
metadata.dc.identifier.url: http://www.malariajournal.com/content/pdf/1475-2875-9-308.pdf
ISSN: 1475-2875 (electronic)
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